Canonical Allele Identifier: CA5168889

Gene: ABCA1

Linked Data

• ClinVar Variation Id: 1781938
• ClinVar RCV Id: RCV002415355
• dbSNP Id: rs574002247
• ExAC: 9:107593215 A / G
• gnomAD v2: 9-107593215-A-G
• gnomAD v3: 9-104830934-A-G
• gnomAD v4: 9-104830934-A-G
• MyVariant Identifiers: chr9:g.107593215A>G (hg19) ; chr9:g.104830934A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.104830934A>G , CM000671.2:g.104830934A>G	GRCh38
NC_000009.11:g.107593215A>G , CM000671.1:g.107593215A>G	GRCh37
NC_000009.10:g.106633036A>G	NCBI36
NG_007981.1:g.102222T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374736.8:c.1883T>C MANE Select	ENSP00000363868.3:p.Val628Ala
ENST00000678995.1:c.1883T>C	ENSP00000504612.1:p.Val628Ala
ENST00000374736.7:c.1883T>C	ENSP00000363868.3:p.Val628Ala
ENST00000494467.1:n.56T>C
NM_005502.3:c.1883T>C	NP_005493.2:p.Val628Ala
XM_005251773.1:c.1883T>C	XP_005251830.1:p.Val628Ala
XM_005251776.1:c.1703T>C	XP_005251833.1:p.Val568Ala
XM_011518339.1:c.1958T>C	XP_011516641.1:p.Val653Ala
XM_011518340.1:c.1958T>C	XP_011516642.1:p.Val653Ala
XM_011518341.1:c.1958T>C	XP_011516643.1:p.Val653Ala
XM_011518342.1:c.1520T>C	XP_011516644.1:p.Val507Ala
XM_011518343.1:c.1958T>C	XP_011516645.1:p.Val653Ala
XM_011518344.1:c.1958T>C	XP_011516646.1:p.Val653Ala
XM_005251773.3:c.1883T>C	XP_005251830.1:p.Val628Ala
XM_005251776.3:c.1703T>C	XP_005251833.1:p.Val568Ala
XM_011518339.3:c.1958T>C	XP_011516641.1:p.Val653Ala
XM_011518340.3:c.1958T>C	XP_011516642.1:p.Val653Ala
XM_011518341.3:c.1958T>C	XP_011516643.1:p.Val653Ala
XM_011518342.3:c.1520T>C	XP_011516644.1:p.Val507Ala
XM_011518344.2:c.1958T>C	XP_011516646.1:p.Val653Ala
XM_017014378.2:c.1958T>C	XP_016869867.1:p.Val653Ala
XM_017014379.2:c.1958T>C	XP_016869868.1:p.Val653Ala
XM_017014380.2:c.1958T>C	XP_016869869.1:p.Val653Ala
XM_017014381.2:c.1958T>C	XP_016869870.1:p.Val653Ala
XM_017014382.2:c.1820T>C	XP_016869871.1:p.Val607Ala
XR_001746223.1:n.2271T>C
NM_005502.4:c.1883T>C MANE Select	NP_005493.2:p.Val628Ala